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Elisa Negroni

Showing results (41-50 of 46) with videos related to

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Human Molecular Genetics|January 17, 2019
Pharmacological modulation of the ER stress response ameliorates oculopharyngeal muscular dystrophyAlberto Malerba, Fanny Roth, Pradeep Harish, et al.
The American Journal of Pathology|August 9, 2012
Generation of isogenic D4Z4 contracted and noncontracted immortal muscle cell clones from a mosaic patient: a cellular model for FSHDYvonne D Krom, Julie Dumonceaux, Kamel Mamchaoui, et al.
Acta Neuropathologica|October 5, 2022
Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophyFanny Roth, Jamila Dhiab, Alexis Boulinguiez, et al.
Skeletal Muscle|November 2, 2011
Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disordersKamel Mamchaoui, Capucine Trollet, Anne Bigot, et al.
Human Molecular Genetics|March 9, 2010
Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibresCapucine Trollet, Seyed Yahya Anvar, Andrea Venema, et al.
Skeletal Muscle|December 15, 2015
CD49d is a disease progression biomarker and a potential target for immunotherapy in Duchenne muscular dystrophyFernanda Pinto-Mariz, Luciana Rodrigues Carvalho, Alexandra Prufer De Queiroz Campos Araujo, et al.
Pageof 5

Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Human Molecular Genetics|January 17, 2019
Pharmacological modulation of the ER stress response ameliorates oculopharyngeal muscular dystrophyAlberto Malerba, Fanny Roth, Pradeep Harish, et al.
The American Journal of Pathology|August 9, 2012
Generation of isogenic D4Z4 contracted and noncontracted immortal muscle cell clones from a mosaic patient: a cellular model for FSHDYvonne D Krom, Julie Dumonceaux, Kamel Mamchaoui, et al.
Acta Neuropathologica|October 5, 2022
Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophyFanny Roth, Jamila Dhiab, Alexis Boulinguiez, et al.
Skeletal Muscle|November 2, 2011
Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disordersKamel Mamchaoui, Capucine Trollet, Anne Bigot, et al.
Human Molecular Genetics|March 9, 2010
Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibresCapucine Trollet, Seyed Yahya Anvar, Andrea Venema, et al.
Skeletal Muscle|December 15, 2015
CD49d is a disease progression biomarker and a potential target for immunotherapy in Duchenne muscular dystrophyFernanda Pinto-Mariz, Luciana Rodrigues Carvalho, Alexandra Prufer De Queiroz Campos Araujo, et al.
Pageof 5